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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903403Generated: October 25, 2026

Sodium hydride → Oxadixyl

https://huagongshe.com/reaction/1903403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloroethyl 2-(methoxyacetyl)-2-(2,6-dimethylphenyl)-hydrazinecarboxylateHCID 20454494—
SolventTolueneHCID 1140—
ProductOxadixylHCID 53735—

Reaction Steps

11.8 g (0.0375 mol) 2-Chloroethyl 2-(methoxyacetyl)-2-(2,6-dimethylphenyl)-hydrazinecarboxylate are added portion-wise to a suspension of 2.0 g sodium hydride (in form of about 55% by weight in mineral oil) in 100 ml absolute toluene at room temperature under a blanket of nitrogen. The reaction temperature rises gradually during this addition up to 40°. After the addtion is complete the mixture is stirred during 30 minutes without cooling and afterwards cooled to 10°. The unreacted sodium hydride is then destroyed with ethanol, the obtained solution washed with water dried with MgSO4 and the solvent removed in vacuo to give the end title compound which is recrystallised from ethanol to yield the title compound as colourless crystals, m.p. 103°-104°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436744
Source datasetuspto-grants-1984_03
ORD IDord-2db8b758f6d7426bb3f09d9ae496eba8
Source noteuspto-grants-1984_03